Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2. - Wikidata - awgldk - TriplyDB

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

http://www.wikidata.org/entity/Q30810767

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Association between the p.V37I variant of GJB2 and hearing loss: a pedigree and meta-analysis.

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P2860

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

http://www.wikidata.org/entity/Q30810767

description

2016 nî lūn-bûn

@nan

2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@ast

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@en

type

label

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@ast

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@en

prefLabel

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@ast

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@en

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Scientific Reports

P1476

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.

@en

P2093

Changling Sun

http://www.w3.org/2001/XMLSchema#string

Hao Wu

http://www.w3.org/2001/XMLSchema#string

Lei Li

http://www.w3.org/2001/XMLSchema#string

Ling Mei

http://www.w3.org/2001/XMLSchema#string

Lingxiang Hu

http://www.w3.org/2001/XMLSchema#string

Tao Yang

http://www.w3.org/2001/XMLSchema#string

Xin Lin

http://www.w3.org/2001/XMLSchema#string

Xueling Wang

http://www.w3.org/2001/XMLSchema#string

Ying Chen

http://www.w3.org/2001/XMLSchema#string

Zhiwu Huang

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome

A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project

Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss.

Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89

Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness.

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P2888

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33279

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scholarly article

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10.1038/SREP33279

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6

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2016-09-13T00:00:00Z

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1002223223

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27623246

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